Allele Registry

Canonical Allele Identifier: PA2826224076

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV001941410

ClinVar Variation:

1442038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Ser112Cys	CA379960501 NM_001198552.2:c.334A>T CA2573146222 NM_001198552.2:c.333_334delinsAT